A Case of Immune Thrombocytopenic Purpura Developing after Treatment for Non-Hodgkin's Lymphoma
Hui-Young Lee, Dae Joon Jeong, Dong Gyu Lee, Kwang-Jin Chun, Sook Won Ryu, Seo‐Young Song
Abstract
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Hui-Young Lee, Dae Joon Jeong, Dong Gyu Lee, Kwang-Jin Chun, Sook Won Ryu, Seo‐Young Song
Abstract
Open-access reader
Immune thrombocytopenic purpura (ITP) can be classified as primary or secondary according to the presence of an underlying non-malignant or malignant disorder, including lymphoproliferative disorders.The estimated prevalence of ITP in patients with Hodgkin's lymphoma is about 1%, and its clinical course has been reported in approximately 50 patients.ITP is an unusual and poorly documented complication in patients with non-Hodgkin's lymphoma.Some cases have been described in patients who have undergone high-dose chemotherapy and autologous bone marrow/peripheral blood stem cell transplantation.Rare cases appear to be coincidental.Here, we report on a rare case of a 61-year-old man who had ITP after being in a state of complete remission of non-Hodgkin's lymphoma for about 15 months.(
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Immune thrombocytopenic purpura (ITP) can be classified as primary or secondary according to the presence of an underlying non-malignant or malignant disorder, including lymphoproliferative disorders.The estimated prevalence of ITP in patients with Hodgkin's lymphoma is about 1%, and its clinical course has been reported in approximately 50 patients.ITP is an unusual and poorly documented complication in patients with non-Hodgkin's lymphoma.Some cases have been described in patients who have undergone high-dose chemotherapy and autologous bone marrow/peripheral blood stem cell transplantation.Rare cases appear to be coincidental.Here, we report on a rare case of a 61-year-old man who had ITP after being in a state of complete remission of non-Hodgkin's lymphoma for about 15 months.(
Key concepts: Medicine, Thrombocytopenic purpura, Lymphoma, Lymphoproliferative disorders, Complication, Chemotherapy, Immune system, Bone marrow